A citation-based method for searching scientific literature

Ashley Pacheco, Ralph Berger, Robert Freedman, Amanda J Law. Sci Rep 2019
Times Cited: 11







List of co-cited articles
82 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity



An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease.
Arne De Roeck, Lena Duchateau, Jasper Van Dongen, Rita Cacace, Maria Bjerke, Tobi Van den Bossche, Patrick Cras, Rik Vandenberghe, Peter P De Deyn, Sebastiaan Engelborghs,[...]. Acta Neuropathol 2018
33
36

Characterization of a REST-Regulated Internal Promoter in the Schizophrenia Genome-Wide Associated Gene MIR137.
Alix Warburton, Gerome Breen, Dan Rujescu, Vivien J Bubb, John P Quinn. Schizophr Bull 2015
27
36


Analysis of miR-137 expression and rs1625579 in dorsolateral prefrontal cortex.
Ilaria Guella, Adolfo Sequeira, Brandi Rollins, Linda Morgan, Federica Torri, Theo G M van Erp, Richard M Myers, Jack David Barchas, Alan F Schatzberg, Stanley J Watson,[...]. J Psychiatr Res 2013
90
27



A human-specific AS3MT isoform and BORCS7 are molecular risk factors in the 10q24.32 schizophrenia-associated locus.
Ming Li, Andrew E Jaffe, Richard E Straub, Ran Tao, Joo Heon Shin, Yanhong Wang, Qiang Chen, Chao Li, Yankai Jia, Kazutaka Ohi,[...]. Nat Med 2016
97
27



Human-specific tandem repeat expansion and differential gene expression during primate evolution.
Arvis Sulovari, Ruiyang Li, Peter A Audano, David Porubsky, Mitchell R Vollger, Glennis A Logsdon, Wesley C Warren, Alex A Pollen, Mark J P Chaisson, Evan E Eichler. Proc Natl Acad Sci U S A 2019
31
27

Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Stephan Ripke, Colm O'Dushlaine, Kimberly Chambert, Jennifer L Moran, Anna K Kähler, Susanne Akterin, Sarah E Bergen, Ann L Collins, James J Crowley, Menachem Fromer,[...]. Nat Genet 2013
18

MicroRNA-137 represses Klf4 and Tbx3 during differentiation of mouse embryonic stem cells.
Ke Jiang, Chunyan Ren, Venugopalan D Nair. Stem Cell Res 2013
30
18

Biological validation of increased schizophrenia risk with NRG1, ERBB4, and AKT1 epistasis via functional neuroimaging in healthy controls.
Kristin K Nicodemus, Amanda J Law, Eugenia Radulescu, Augustin Luna, Bhaskar Kolachana, Radhakrishna Vakkalanka, Dan Rujescu, Ina Giegling, Richard E Straub, Kate McGee,[...]. Arch Gen Psychiatry 2010
99
18

Effects of MIR137 on fronto-amygdala functional connectivity.
Omar Mothersill, Derek W Morris, Sinead Kelly, Emma Jane Rose, Ciara Fahey, Carol O'Brien, Ronan Lyne, Richard Reilly, Michael Gill, Aiden P Corvin,[...]. Neuroimage 2014
37
18


Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability.
Marjolein H Willemsen, Astrid Vallès, Laurens A M H Kirkels, Mathilde Mastebroek, Nikkie Olde Loohuis, Aron Kos, Willemijn M Wissink-Lindhout, Arjan P M de Brouwer, Willy M Nillesen, Rolph Pfundt,[...]. J Med Genet 2011
111
18

Transcriptional targets of the schizophrenia risk gene MIR137.
A L Collins, Y Kim, R J Bloom, S N Kelada, P Sethupathy, P F Sullivan. Transl Psychiatry 2014
38
18

Genetic insights into the neurodevelopmental origins of schizophrenia.
Rebecca Birnbaum, Daniel R Weinberger. Nat Rev Neurosci 2017
196
18

New Repeat Polymorphism in the AKT1 Gene Predicts Striatal Dopamine D2/D3 Receptor Availability and Stimulant-Induced Dopamine Release in the Healthy Human Brain.
Elena Shumay, Corinde E Wiers, Ehsan Shokri-Kojori, Sung Won Kim, Colin A Hodgkinson, Hui Sun, Dardo Tomasi, Christopher T Wong, Daniel R Weinberger, Gene-Jack Wang,[...]. J Neurosci 2017
11
18


The schizophrenia risk gene product miR-137 alters presynaptic plasticity.
Sandra Siegert, Jinsoo Seo, Ester J Kwon, Andrii Rudenko, Sukhee Cho, Wenyuan Wang, Zachary Flood, Anthony J Martorell, Maria Ericsson, Alison E Mungenast,[...]. Nat Neurosci 2015
124
18

Experimental validation of candidate schizophrenia gene ZNF804A as target for hsa-miR-137.
Albert H Kim, Erin K Parker, Vernell Williamson, Gowon O McMichael, Ayman H Fanous, Vladimir I Vladimirov. Schizophr Res 2012
78
18

The impact of genome wide supported microRNA-137 (MIR137) risk variants on frontal and striatal white matter integrity, neurocognitive functioning, and negative symptoms in schizophrenia.
Carissa Nadia Kuswanto, Min Yi Sum, Anqi Qiu, Yih-Yian Sitoh, Jianjun Liu, Kang Sim. Am J Med Genet B Neuropsychiatr Genet 2015
35
18

The impact of MIR137 on dorsolateral prefrontal-hippocampal functional connectivity in healthy subjects.
Bing Liu, Xiaolong Zhang, Bing Hou, Jin Li, Chengxiang Qiu, Wen Qin, Chunshui Yu, Tianzi Jiang. Neuropsychopharmacology 2014
43
18

Transgenic mice overexpressing miR-137 in the brain show schizophrenia-associated behavioral deficits and transcriptome profiles.
Yuuichi Arakawa, Kazumasa Yokoyama, Shinya Tasaki, Junichi Kato, Kosuke Nakashima, Michiyasu Takeyama, Atsushi Nakatani, Motohisa Suzuki. PLoS One 2019
10
20

Partial loss of psychiatric risk gene Mir137 in mice causes repetitive behavior and impairs sociability and learning via increased Pde10a.
Ying Cheng, Zhi-Meng Wang, Weiqi Tan, Xiaona Wang, Yujing Li, Bing Bai, Yuxin Li, Shuang-Feng Zhang, Hai-Liang Yan, Zuo-Lun Chen,[...]. Nat Neurosci 2018
62
18


Schizophrenia miR-137 locus risk genotype is associated with dorsolateral prefrontal cortex hyperactivation.
Theo G M van Erp, Ilaria Guella, Marquis P Vawter, Jessica Turner, Gregory G Brown, Gregory McCarthy, Douglas N Greve, Gary H Glover, Vince D Calhoun, Kelvin O Lim,[...]. Biol Psychiatry 2014
56
18

The genome-wide supported microRNA-137 variant predicts phenotypic heterogeneity within schizophrenia.
T A Lett, M M Chakravarty, D Felsky, E J Brandl, A K Tiwari, V F Gonçalves, T K Rajji, Z J Daskalakis, H Y Meltzer, J A Lieberman,[...]. Mol Psychiatry 2013
88
18

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere,[...]. Nat Genet 2018
638
18

Integrative analysis of 111 reference human epigenomes.
Anshul Kundaje, Wouter Meuleman, Jason Ernst, Misha Bilenky, Angela Yen, Alireza Heravi-Moussavi, Pouya Kheradpour, Zhizhuo Zhang, Jianrong Wang, Michael J Ziller,[...]. Nature 2015
18

Beyond GWASs: illuminating the dark road from association to function.
Stacey L Edwards, Jonathan Beesley, Juliet D French, Alison M Dunning. Am J Hum Genet 2013
445
18

A direct characterization of human mutation based on microsatellites.
James X Sun, Agnar Helgason, Gisli Masson, Sigríður Sunna Ebenesersdóttir, Heng Li, Swapan Mallick, Sante Gnerre, Nick Patterson, Augustine Kong, David Reich,[...]. Nat Genet 2012
178
18

MAOA Variants and Genetic Susceptibility to Major Psychiatric Disorders.
Zichao Liu, Liang Huang, Xiong-Jian Luo, Lichuan Wu, Ming Li. Mol Neurobiol 2016
24
18

The genome-wide risk alleles for psychiatric disorders at 3p21.1 show convergent effects on mRNA expression, cognitive function, and mushroom dendritic spine.
Zhihui Yang, Danyang Zhou, Huijuan Li, Xin Cai, Weipeng Liu, Lu Wang, Hong Chang, Ming Li, Xiao Xiao. Mol Psychiatry 2020
31
18

Linkage disequilibrium between STRPs and SNPs across the human genome.
Bret A Payseur, Michael Place, James L Weber. Am J Hum Genet 2008
25
18


An integrated map of structural variation in 2,504 human genomes.
Peter H Sudmant, Tobias Rausch, Eugene J Gardner, Robert E Handsaker, Alexej Abyzov, John Huddleston, Yan Zhang, Kai Ye, Goo Jun, Markus Hsi-Yang Fritz,[...]. Nature 2015
18

10 Years of GWAS Discovery: Biology, Function, and Translation.
Peter M Visscher, Naomi R Wray, Qian Zhang, Pamela Sklar, Mark I McCarthy, Matthew A Brown, Jian Yang. Am J Hum Genet 2017
18

The genetics of bipolar disorder.
Francis James A Gordovez, Francis J McMahon. Mol Psychiatry 2020
49
18

A cis-phase interaction study of genetic variants within the MAOA gene in major depressive disorder.
JieXu Zhang, YanBo Chen, KeRang Zhang, Hong Yang, Yan Sun, Yue Fang, Yan Shen, Qi Xu. Biol Psychiatry 2010
36
18

Finding the missing heritability of complex diseases.
Teri A Manolio, Francis S Collins, Nancy J Cox, David B Goldstein, Lucia A Hindorff, David J Hunter, Mark I McCarthy, Erin M Ramos, Lon R Cardon, Aravinda Chakravarti,[...]. Nature 2009
18

Evidence of biologic epistasis between BDNF and SLC6A4 and implications for depression.
L Pezawas, A Meyer-Lindenberg, A L Goldman, B A Verchinski, G Chen, B S Kolachana, M F Egan, V S Mattay, A R Hariri, D R Weinberger. Mol Psychiatry 2008
181
18

Disease-Associated Short Tandem Repeats Co-localize with Chromatin Domain Boundaries.
James H Sun, Linda Zhou, Daniel J Emerson, Sai A Phyo, Katelyn R Titus, Wanfeng Gong, Thomas G Gilgenast, Jonathan A Beagan, Beverly L Davidson, Flora Tassone,[...]. Cell 2018
83
18


A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
18

Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
18


miR-124 and miR-137 inhibit proliferation of glioblastoma multiforme cells and induce differentiation of brain tumor stem cells.
Joachim Silber, Daniel A Lim, Claudia Petritsch, Anders I Persson, Alika K Maunakea, Mamie Yu, Scott R Vandenberg, David G Ginzinger, C David James, Joseph F Costello,[...]. BMC Med 2008
711
18


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.